The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

子宫内膜异位症 生物 共病 生物信息学 医学 内科学 遗传学
作者
Nilüfer Rahmioğlu,Sally Mortlock,Marzieh Ghiasi,Peter Möller,Lilja Stefánsdóttir,Geneviève Galarneau,Constance Turman,Rebecca Danning,Matthew H. Law,Yadav Sapkota,Paraskevi Christofidou,Sini Skarp,Ayush Giri,Karina Banasik,Michał Krassowski,Maarja Lepamets,Błażej Marciniak,Margit Nõukas,Danielle Perro,Eeva Sliz
出处
期刊:Nature Genetics [Nature Portfolio]
卷期号:55 (3): 423-436 被引量:255
标识
DOI:10.1038/s41588-023-01323-z
摘要

Endometriosis is a common condition associated with debilitating pelvic pain and infertility. A genome-wide association study meta-analysis, including 60,674 cases and 701,926 controls of European and East Asian descent, identified 42 genome-wide significant loci comprising 49 distinct association signals. Effect sizes were largest for stage 3/4 disease, driven by ovarian endometriosis. Identified signals explained up to 5.01% of disease variance and regulated expression or methylation of genes in endometrium and blood, many of which were associated with pain perception/maintenance (SRP14/BMF, GDAP1, MLLT10, BSN and NGF). We observed significant genetic correlations between endometriosis and 11 pain conditions, including migraine, back and multisite chronic pain (MCP), as well as inflammatory conditions, including asthma and osteoarthritis. Multitrait genetic analyses identified substantial sharing of variants associated with endometriosis and MCP/migraine. Targeted investigations of genetically regulated mechanisms shared between endometriosis and other pain conditions are needed to aid the development of new treatments and facilitate early symptomatic intervention. Meta-analyses of genome-wide association studies for endometriosis identify 49 distinct association signals. Fine-mapping of causal variants explores functional effects across various tissues. Genetic correlations between endometriosis and other pain conditions are also highlighted.
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